About this trial
This is an open-label, multicentre, randomized phase II non-inferiority trial aiming to compare the efficacy and safety of 4 versus 6 cycles of CHP (administered at 21-day intervals), both in combination with 6 cycles of polatuzumab vedotin and rituximab, in previously untreated patients with diffuse large B-cell lymphoma (DLBCL) and an International Prognostic Index (IPI) score of 0-1. The study's primary objective is to determine if shorter CHP duration can achieve comparable outcomes to the standard 6-cycle regimen when combined with polatuzumab vedotin and rituximab
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Newly diagnosed, untreated, biopsy-proven CD20 positive diffuse large B-cell lymphoma (DLBCL)
Age ≥18yo and ≤80yo at the time of signing consent
International Prognostic Index (IPI) score 0-1
ECOG 0-2
Disqualifiers
Patients with central nervous system or primary mediastinal lymphoma, and patients with transformed lymphoma.
Patients with uncontrolled cardiovascular and cerebrovascular diseases, coagulation disorders, connective tissue diseases, severe infectious diseases, etc.
Pregnant or lactating women.
Known history of human immunodeficiency virus (HIV) or active hepatitis C virus (HCV; positive by RNA polymerase chain reaction [PCR]) infection.
Trial design
Parallel
Treatments tested in this trial
Polatuzumab Vedotin
DrugPolatuzumab vedotin IV infusion will be administered as per the schedule specified in the respective arm.
Rituximab
DrugRituximab IV infusion will be administered as per the schedule specified in the respective arm.
Cyclophosphamide
DrugCyclophosphamide IV infusion will be administered as per the schedule specified in the respective arm
Doxorubicin
DrugDoxorubicin IV infusion will be administered as per the schedule specified in the respective arm.
Prednisone
DrugPrednisone PO will be administered as per the schedule specified in the respective arm.
Treatment groups
Trial outcomes
Primary outcomes
Complete response rate (CR)
To assess the complete response rate (CR) at the end of treatment with Treatment
Secondary outcomes
Overall Response Rate (ORR)
Objective Response Rate (ORR) is defined as the proportion of subjects who achieve CR or PR after treatment
Duration of Response (DoR)
The length of time between the achievement of criteria for response to treatment (first documented complete or partial response) and the first documented relapse or progression.
Progression-free survival (PFS)
The time from the enrollment of a subject to the occurrence of (in any way) progression of disease or Death for any reason. patients with indeterminate recurrence or Death at the last follow-up, defined as the date of the last Investigation
To identify biomarkers
To identify biomarkers that may predict response to a combination regimen, biomarkers associated with progression to a more severe disease state, biomarkers that are sensitive to the development of Adverse event, biomarkers that provide evidence of the activity of the combination, or biomarkers that may enhance the understanding or understanding of the biology of the disease.
Sponsors and contacts
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